US3294710A - Flameproof polyurethane resins - Google Patents

Flameproof polyurethane resins Download PDF

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Publication number
US3294710A
US3294710A US213142A US21314262A US3294710A US 3294710 A US3294710 A US 3294710A US 213142 A US213142 A US 213142A US 21314262 A US21314262 A US 21314262A US 3294710 A US3294710 A US 3294710A
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US
United States
Prior art keywords
compounds
foam
component
chlorinated
fyrol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US213142A
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English (en)
Inventor
Richard H Rosenberg
Robert S Cooper
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Stauffer Chemical Co
Original Assignee
Stauffer Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to NL136657D priority Critical patent/NL136657C/xx
Priority to NL295929D priority patent/NL295929A/xx
Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co
Priority to US213142A priority patent/US3294710A/en
Priority to GB27161/63A priority patent/GB1021939A/en
Priority to FR941779A priority patent/FR1388667A/fr
Priority to DE19631745471 priority patent/DE1745471A1/de
Priority to DE19631520963 priority patent/DE1520963A1/de
Application granted granted Critical
Publication of US3294710A publication Critical patent/US3294710A/en
Priority to NL727211014A priority patent/NL146514B/xx
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/40—Esters thereof
    • C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/28—Phosphorus compounds with one or more P—C bonds
    • C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
    • C07F9/40—Esters thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30—Low-molecular-weight compounds
    • C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3878—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus
    • C08G18/3889—Low-molecular-weight compounds having heteroatoms other than oxygen having phosphorus having nitrogen in addition to phosphorus
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/50—Polyethers having heteroatoms other than oxygen
    • C08G18/5075—Polyethers having heteroatoms other than oxygen having phosphorus
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04—Polyurethanes
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2110/00—Foam properties
    • C08G2110/0025—Foam properties rigid

Definitions

  • This invention relates to flame resistant polyurethane foams.
  • this invention relates to polyurethane foams which have been made flame resistant by the addition and reaction therewith of a mixture comprising one or more phosphorus containing compounds and a chlorinated hydrocarbon composition.
  • the resulting fiame-proofed compositions may be used in the form of expanded foamed products as thermal insulation.
  • urethane or isocyanate polymers are well-known commercial process, see for instance Kirk- Othmer, The Encyclopedia of Chemical Technology, first supplement, pages 888, et seq. (Interscience, 1957). Briefly, this process involves the reaction of an isocyanate and a second compound which may contain an hydroxyl, amino or carboxy group, i.e., a compound containing active hydrogen.
  • isocyanate material is intended to include isocyanate or urethane compositions containing unreacted NCO radicals.
  • the most common polymers are formed by the reaction of toluene diisocyanate (hereafter TDI) and a saturated polyether or polyester. (This latter compound may, however, contain benzene unsaturation.)
  • Other representative isocyanates include polymethylene polyphenyl isocyanate and p,p-diphenylmethylene diisocyanate.
  • Representative polyesters are the reaction products of adipic acid and/ or phthalic anhydride and ethylene glycol.
  • Other compounds which may be used in place of the polyesters or polyethers are simple glycols, polyglycols, castor oil, drying oils, etc. Whether the products are to be flexible or rigid depends upon thedegree of crosslinking and thus the type of polyol which is used. Since the products of this invention may replace only a part of the polyol, they are thus suitable for use in either flexible or rigid foams.
  • foaming agent as used herein is intended to include both reactive materials such as water and inert materials such as halohydrocarbons, or mixtures of the two, which cause the copolymers to form an expanded foam.
  • the abovedescribed urethane polymers may be flameproofed by adding a combination of at least two flameproofing agents.
  • This combination produces results in the final polyurethane foam which are far better than would be expected from an examination of the results which are obtained by the use of either of the flameproofing components alone.
  • this invention covers the use of a phosphorus containing flameproofing component and a chlorinated hydrocarbon flameproofing component.
  • the phosphorus containing compounds in turn fall into two separate classes.
  • the first class of compounds may be represented by the general formula:
  • RO R ort wherein R and R may be the same or different alkyl or haloalkyl radicals and R and R may be the same or different lower alkylene radicals and R is a lower alkylene radical.
  • this reaction may be said to involve the reaction of a dialkanolamine, an aldehyde or ketone, and a dialkyl phosphite.
  • Suitable dialkanolamines for the purpose of this invention include such compounds as diethanolamine, dipropanola-mine, ethanol propanolamine, dibutanolamine, dioctonalamine, etc.
  • Suitable aldehydes or ketones are such well-known compounds as formaldehyde, acetaldehyde, butyraldehyde, furfural, acetone, methyl ethyl ketone, etc.
  • Dialkyl phosphites which are suitable are dimethyl phosphite, diethyl phosphite, methyl ethyl phosphite, dipropyl phosphite, dibutyl phosphite, dioctyl phosphite, beta chloroethyl phosphite, etc.
  • Example 1 Preparazi0vz of diethyl N,N-diethan0lamin0- methylphosphonate To 30.9 grams of diethanolamine was added 24.4 grams of aqueous 37% formaldehyde while stirring at 2030 C. in a reaction flask equipped with thermometer, and dropping funnel. Diethyl phosphite, 41.4 grams, was then added dropwise while stirring and holding the temperature at 2135 C. Both of the above reactions were exothermic. The reaction mixture was held at 35 C. with cooling until the exothermic reaction was complete in about 40 minutes and was then cooled below 30 C. The mixture was further stirred at room temperature and After cooling it was extracted with ml. of ether and the resulting aqueous phase was then concentrated by distillation under reduced pressure.
  • R, R, and x are as defined above. It is understood, of course, that the x moles of alkylene oxide do not necessarily react symmetrically with the acidic hydrogens of the phosphorus acid.
  • Suitable phosphoric acids are mono alkyl phosphoric acids such as methyl phosphoric acid, ethyl phosphoric acid, butyl phosphoric acid, lauryl phosphoric acid, etc.
  • Suitable mono aryl phosphoric acids are phenyl phosphoric acid, cresyl phosphoric acid, xylyl phosphoric acid, etc.
  • Phosphonic acids which may be used are alkyl phosphonic acids such as methylphospho-nic acid, ethylphosphonic acid and butylphosphonic acid; chloroalkylphosphonic acids such as chloromethylphosphonic acid and trichloromethylphosphonic acid; arylphosphonic acids such as phenylphosphonic acid and cresylphosphonic acid; hydroxyalkylphosphonic acids such as hydroxyrnethylphosphonic acid; and alkanolaminoalkylphosphonic acids such as diethanol aminomethylphosphonic acid.
  • alkyl phosphonic acids such as methylphospho-nic acid, ethylphosphonic acid and butylphosphonic acid
  • chloroalkylphosphonic acids such as chloromethylphosphonic acid and trichloromethylphosphonic acid
  • arylphosphonic acids such as phenylphosphonic acid and cresylphosphonic acid
  • hydroxyalkylphosphonic acids such as hydroxyrnethylphosphonic acid
  • Suitable alkylene oxides which may be used are ethylene oxide, propylene oxides, butylene oxide and the like.
  • the chlorinated hydrocarbons which are used in the practice of the present invention consist of two basic types of materials,.namely, the chlorinated paraflins and the chlorinated polyphenyls.
  • these compounds should contain at least 60% chlorine and be solid compounds with melting points above approximately 100 C. Compounds meeting these general specifications will remain in the final urethane composition without migration or bleeding such as may occur when the less chlorinated liquid products are used.
  • the chlorinated paraffins are chlorinated derivatives of naturally occurring higher parafiin's. They are wellknown commercial products and when they contain at least 60% chlorine, as is preferred for the present invention, they are solid products. They are prepared by passing chlorine through molten parafiin wax, in some instances, using a hydrocarbon solvent in order to obtain the high chlorine content.
  • suitable commercial products see for instance the Encyclopedia of Chemical Technology, Kirk-Othmer, Interscience, 1949, vol. 3, pages 781, et seq. Table I, in particular, shows a list of products of the type suitable for the present invention.
  • the chlorinated polyphenyls suitable for this invention are chemically inert materials prepared by the chlorination of diphenyl, terphenyl, or the more complex polyphenyls.
  • the pure compounds are usually crystalline solids but the commercial products are more generally mixtures of the various compounds and, in some cases, may be viscous liquids. Usually when at least 60% chlorine is present, as is preferred for the present invention, the products are at least partly of a crystalline nature.
  • a number of commercially available products are satisfactory for the purpose of this invention and such compounds and their method of manufacture are clearly described in Kirk-Othrner, supra, at pages 826, et seq. Table I, in particular shows the physical properties of such compounds.
  • component A was weighed into a 350 ml. stainless steel beaker, blended by hand, and then stirred with a 1750 rpm. mechanical stirrer having two three-bladed propellers 2 inches in diameter.
  • component B were similarly weighed and mixed in a 16-ounce plastic impregnated paper cup.
  • Component A was poured into component B and the blend stirred with the same mixer for 15 seconds.
  • the mixture was then poured to a room temperature, paper lined mold where it reacted releasing heat, foamed, and polymerized to a low density cellular thermo-setting plastic having essentially closed cells filled with the foaming agent vapors.
  • chlorinated hydrocarbons were used in these examples, they were dissolved in the B component prior to final mixing.
  • test used was that which is designated as ASTM D1692-59T. This procedure is outlined as follows:
  • Specimens were cut from various parts of the foam block. They were trimmed on a bandsaw to /2 x 6" x 2 dimensions. Marks were made on top of the specimens 1" from the 2" wide ends. The specimens were rested on a piece of A" hardware cloth (galvanized steel woven Wire screen having mesh openings approximately A" squares) which measured 3" x 8". One 3" end of the screen was bent up for /2". The 2" end of the foam sample was placed against this turned-up end. The screen and sample were placed in a draft-free chamber. A Bunsen burner with a wing tip which had a 1 /2 high 5 flame was placed /2" below the turned-up screen end.
  • a Bunsen burner with a wing tip which had a 1 /2 high 5 flame was placed /2" below the turned-up screen end.
  • the gas burner was turned off and a stopwatch was started. The watch was stopped when the flame went out or reached the second mark on the top of the specimen. The time interval and the length of the foam charred or burned (measured on the top of the specimen from the first one inch mark) were recorded. A minimum of ten tests was run on each foam. The test specifications established the criteria for rating the foams as non-burning (never reaching the first one inch mark), self-extinguishing (went out before reaching the second mark), or burning.
  • Percenbages are based on total ingredients except the foaming agent in this and all the following formulations.
  • Sucrose base polyether polyol obtained by condensing sucrose with propylene oxide.
  • Component B is a compound having Component B:
  • This foam contained 2.16% P.
  • Polyether polyol obtained by condensing sucrose with propylene oxide.
  • Component B is a compound having Component B:
  • Component B is a compound having Component B:
  • Component B is a compound having Component B:
  • Chlorowax 70 LP Component B
  • Component B is a compound having Component B:
  • This foam contained 1.45% P.
  • Component B Y selectron 6403 (28.9% NCO) 135.0
  • Example I5.Foamcontaining 20% Chlorowax 70 LP Component A: Gm. Selectron 6402 (H.N. 469) 37.7 Silicone L-521 0.5
  • Component B is a compound having Component B:
  • chlorinated hydrocarbons which are generally solids with melting points above 100 C., prevents migration or bleeding as may often occur when liquid plasticizer-type self-extinguishing agents are used.
  • a flame resistant urethane composition comprising:
  • a phosphorus compound selected from the class consisting of (1) a dialkanolaminoalkylphosphonate having the formula:
  • R is a member of the class consisting of alkyl, aryl, alkoxy, aryloxy, chloroalkyl, hydroxy alkyl and alkanolaminoalkyl;
  • R and R" are lower alkylene radicals; and x and y may vary from about 1 to about 4; in an amount suificient to provide about 0.75% to about 1.75 phosphorus in the final composition;
  • a chlorinated hydrocarbon selected from the class consisting of chlorinated paraffins and chlorinated polyphenyls in an amount sutficient to provide about 5% to about 10% chlorine in the final composition
  • a flame resistant urethane composition according to claim 1 wherein the phosphorus compound is diethyl N,N-diethanolaminomethylphosphonate.
  • a flame resistant urethane composition according to claim 1 wherein the phosphorus compound is polyoxypropylene phenylphosphonate.
  • a flame resistant urethane composition according to claim 1 wherein the phosphorus compound is polyoxypropylene monochloromethylphosphonate.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Fireproofing Substances (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US213142A 1962-07-30 1962-07-30 Flameproof polyurethane resins Expired - Lifetime US3294710A (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
NL136657D NL136657C (de) 1962-07-30
NL295929D NL295929A (de) 1962-07-30
US213142A US3294710A (en) 1962-07-30 1962-07-30 Flameproof polyurethane resins
GB27161/63A GB1021939A (en) 1962-07-30 1963-07-09 Flame-resistant polyurethane compositions
FR941779A FR1388667A (fr) 1962-07-30 1963-07-17 Résines polyuréthanes ininflammables, leur procédé de fabrication et leurs applications
DE19631745471 DE1745471A1 (de) 1962-07-30 1963-07-24 Verfahren zum Herstellen feuerbestaendiger Polyurethan-Harze
DE19631520963 DE1520963A1 (de) 1962-07-30 1963-07-27 Feuerbestaendige Polyurethan-Schaeume
NL727211014A NL146514B (nl) 1962-07-30 1972-08-11 Werkwijze voor de bereiding van een eventueel geschuimd vlamvast urethaanmateriaal onder toepassing van een fosfor bevattende polyol.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US213142A US3294710A (en) 1962-07-30 1962-07-30 Flameproof polyurethane resins

Publications (1)

Publication Number Publication Date
US3294710A true US3294710A (en) 1966-12-27

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US213142A Expired - Lifetime US3294710A (en) 1962-07-30 1962-07-30 Flameproof polyurethane resins

Country Status (4)

Country Link
US (1) US3294710A (de)
DE (2) DE1745471A1 (de)
GB (1) GB1021939A (de)
NL (2) NL136657C (de)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3422046A (en) * 1966-02-03 1969-01-14 Sherwin Williams Co Coating containing a condensate of a phosphate ether polyol and a melamine,an alkylated amine,and a halogenated hydrocarbon
US3440211A (en) * 1966-07-27 1969-04-22 Du Pont Flame retardant nylon composition
US3518262A (en) * 1966-08-12 1970-06-30 Monsanto Co Diorgano-aminomethylphosphine sulfides and process
US3539536A (en) * 1965-10-23 1970-11-10 Stauffer Chemical Co Flame resistant polyurethane compositions from bis-(hydroxypolyalkoxyalkyl)aminomethylphosphonates
DE2036592A1 (de) * 1970-07-23 1972-01-27 Knapsack Ag Schwer entflammbare Polyurethane sowie Verfahren zu deren Herstellung
US3684754A (en) * 1970-05-19 1972-08-15 Gulf Research Development Co Flame-retarded polyurethane compositions comprising a phosphorus-containing polyol and an aromatic carboxylic acid
FR2281376A1 (fr) * 1974-08-05 1976-03-05 Stauffer Chemical Co Synthese de l'hydroxymethylphosphonate de di-polyoxyethylene
US3956200A (en) * 1970-10-08 1976-05-11 Stauffer Chemical Company Flame retardant blends for flexible polyurethane foams
US4102830A (en) * 1974-05-13 1978-07-25 Societe Nationale Des Poudres Et Explosifs Diol-phosphonates as flame-retardants in polyurethane foam
US4404313A (en) * 1981-08-31 1983-09-13 Stauffer Chemical Company Flame retardant-smolder resistant textile backcoating
US4444831A (en) * 1981-08-31 1984-04-24 Stauffer Chemical Company Flame retardant-smolder resistant textile backcoating
US5981612A (en) * 1994-12-27 1999-11-09 Basf Aktiengesellschaft Production of flameproofed, rigid, isocyanate-based foams

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551562A (en) * 1946-09-26 1951-05-01 Monsanto Chemicals Compositions consisting essentially of chlorinated meta diphenylbenzene and chlorinated para diphenylbenzene and process of preparing same
DE1106489B (de) * 1959-08-11 1961-05-10 Bayer Ag Verfahren zur Herstellung von Phosphoratome und Urethangruppen enthaltenden, gegebenenfalls verschaeumten Kunststoffen
US3067149A (en) * 1960-05-04 1962-12-04 Nopco Chem Co Stabilization of polyurethane resin foams
US3076010A (en) * 1960-03-25 1963-01-29 Stauffer Chemical Co Bis (hydroxyalkyl) amino alkyl phosphonic acid diesters

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2551562A (en) * 1946-09-26 1951-05-01 Monsanto Chemicals Compositions consisting essentially of chlorinated meta diphenylbenzene and chlorinated para diphenylbenzene and process of preparing same
DE1106489B (de) * 1959-08-11 1961-05-10 Bayer Ag Verfahren zur Herstellung von Phosphoratome und Urethangruppen enthaltenden, gegebenenfalls verschaeumten Kunststoffen
US3076010A (en) * 1960-03-25 1963-01-29 Stauffer Chemical Co Bis (hydroxyalkyl) amino alkyl phosphonic acid diesters
US3067149A (en) * 1960-05-04 1962-12-04 Nopco Chem Co Stabilization of polyurethane resin foams

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3539536A (en) * 1965-10-23 1970-11-10 Stauffer Chemical Co Flame resistant polyurethane compositions from bis-(hydroxypolyalkoxyalkyl)aminomethylphosphonates
US3422046A (en) * 1966-02-03 1969-01-14 Sherwin Williams Co Coating containing a condensate of a phosphate ether polyol and a melamine,an alkylated amine,and a halogenated hydrocarbon
US3440211A (en) * 1966-07-27 1969-04-22 Du Pont Flame retardant nylon composition
US3518262A (en) * 1966-08-12 1970-06-30 Monsanto Co Diorgano-aminomethylphosphine sulfides and process
US3684754A (en) * 1970-05-19 1972-08-15 Gulf Research Development Co Flame-retarded polyurethane compositions comprising a phosphorus-containing polyol and an aromatic carboxylic acid
DE2036592A1 (de) * 1970-07-23 1972-01-27 Knapsack Ag Schwer entflammbare Polyurethane sowie Verfahren zu deren Herstellung
US3956200A (en) * 1970-10-08 1976-05-11 Stauffer Chemical Company Flame retardant blends for flexible polyurethane foams
US4102830A (en) * 1974-05-13 1978-07-25 Societe Nationale Des Poudres Et Explosifs Diol-phosphonates as flame-retardants in polyurethane foam
US3970729A (en) * 1974-08-05 1976-07-20 Stauffer Chemical Company Process of synthesizing di-polyoxylalkylene hydroxymethylphosphonate
FR2281376A1 (fr) * 1974-08-05 1976-03-05 Stauffer Chemical Co Synthese de l'hydroxymethylphosphonate de di-polyoxyethylene
US4404313A (en) * 1981-08-31 1983-09-13 Stauffer Chemical Company Flame retardant-smolder resistant textile backcoating
US4444831A (en) * 1981-08-31 1984-04-24 Stauffer Chemical Company Flame retardant-smolder resistant textile backcoating
US5981612A (en) * 1994-12-27 1999-11-09 Basf Aktiengesellschaft Production of flameproofed, rigid, isocyanate-based foams

Also Published As

Publication number Publication date
DE1745471A1 (de) 1971-09-02
NL136657C (de) 1900-01-01
GB1021939A (en) 1966-03-09
DE1520963A1 (de) 1969-07-03
NL295929A (de) 1900-01-01

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